This mutant allele was engineered to remove the alternative splice site required for the expression of the Cr2 isoform but leave the Cr1 isoform intact. A construct containing a cDNA fusion of the SCRs 18 (thus removing the alternative splice junction) was ligated to the testes specific self-deleting pACN neomycin resistance gene and flanked by Cr2 homologous DNA. This construct replaced exons 1-8 of the endogenous gene. The neomycin selection cassette was removed in the germline. This allele expresses Cr1 on B cells but is deficient for the full length Cr2 protein. An alternative splice within the Cr2 gene created a truncated product that encoded a novel protein termed iCr2 that was expressed on the surface of these cells. (J:223195)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
129
Targeted
Insertion, Intragenic deletion
--
1
5
1

Phenotypes

Legend:
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes:
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Phenotypes

References Literature

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PMID
Journal
Year
IF
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